Genetic modifiers of neurological disease

Curr Opin Genet Dev. 2011 Jun;21(3):349-53. doi: 10.1016/j.gde.2010.12.007. Epub 2011 Jan 19.

Abstract

Genetic modifiers make an important contribution to neurological disease phenotypes. Significant progress has been made by studying genetic modifiers in model organisms. The ability to study complex genetic interactions in model systems contributes to our understanding of the genetic factors that influence neurological disease. This will lead to the development of novel therapeutic strategies and personalized treatment based on genetic risk.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Carrier Proteins / genetics*
  • Charcot-Marie-Tooth Disease / genetics
  • Disease Models, Animal
  • Humans
  • Huntington Disease / genetics
  • Mice
  • Nervous System Diseases / genetics*
  • Phenotype
  • RNA Splicing Factors
  • Rett Syndrome / genetics
  • Spinocerebellar Ataxias / genetics

Substances

  • Carrier Proteins
  • RNA Splicing Factors
  • Scnm1 protein, mouse